Pharmacokinetic PK Analysis Noncompartmental / Compartmental PK/PD

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Nuventra takes a common sense approach to provide excellence in pharmacokinetics and help companies developing pharmaceuticals successfully navigate the drug development process leading to marketing approval. We make clinical pharmacology and pharmacokinetics more accessible for the industry while simultaneously providing robust interpretation of data. Our highly experienced Pharmacokineticists conduct analyses in a fully validated computing environment with the latest PK modeling software.

Noncompartmental (NCA) PK Service Options

Nuventra offers five different options for supporting your program’s clinical PK/PD needs.  All of our service options include noncompartmental clinical PK analysis with turn-around-times as fast as 24 hours.  Reporting options range from simple outputs in SAS Transport Files, Microsoft Word & Excel to robust submission-ready reports.  We will work with you to determine the most appropriate and cost-effective option for your particular program

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Our experience and services includes:

  • Robust pharmacokinetic analysis of data using industry standard validated software
  • Allometric scaling
  • Authoring integrated Clinical/PK study reports or standalone PK reports
  • Preclinical ADME and human studies
  • Toxicokinetic input into toxicology studies and TK data analysis and report writing
  • Data management services for PK data to ensure compliance with current CDISC standards
  • Pharmacodynamic (PD) analysis and reporting
  • PK/PD analysis